AU2001256000B2 - Delamination process - Google Patents
Delamination process Download PDFInfo
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- AU2001256000B2 AU2001256000B2 AU2001256000A AU2001256000A AU2001256000B2 AU 2001256000 B2 AU2001256000 B2 AU 2001256000B2 AU 2001256000 A AU2001256000 A AU 2001256000A AU 2001256000 A AU2001256000 A AU 2001256000A AU 2001256000 B2 AU2001256000 B2 AU 2001256000B2
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- flakes
- metal
- polymeric substrate
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- water
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- 238000000034 method Methods 0.000 title claims description 59
- 230000008569 process Effects 0.000 title claims description 45
- 230000032798 delamination Effects 0.000 title description 4
- 239000000463 material Substances 0.000 claims description 125
- 239000011324 bead Substances 0.000 claims description 55
- 229910052751 metal Inorganic materials 0.000 claims description 49
- 239000002184 metal Substances 0.000 claims description 49
- 239000000758 substrate Substances 0.000 claims description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 238000003801 milling Methods 0.000 claims description 34
- 239000010792 electronic scrap Substances 0.000 claims description 21
- 238000004064 recycling Methods 0.000 claims description 18
- 239000002245 particle Substances 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000008262 pumice Substances 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 6
- 229920003023 plastic Polymers 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 239000002699 waste material Substances 0.000 claims description 5
- 239000012776 electronic material Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 25
- 239000004417 polycarbonate Substances 0.000 description 17
- 229920000515 polycarbonate Polymers 0.000 description 17
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 8
- 239000010931 gold Substances 0.000 description 8
- 229910052737 gold Inorganic materials 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 238000009826 distribution Methods 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000000630 rising effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000010970 precious metal Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000446313 Lamella Species 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003353 gold alloy Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000246 remedial effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B17/00—Recovery of plastics or other constituents of waste material containing plastics
- B29B17/04—Disintegrating plastics, e.g. by milling
- B29B2017/0424—Specific disintegrating techniques; devices therefor
- B29B2017/0472—Balls or rollers in a container
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/52—Mechanical processing of waste for the recovery of materials, e.g. crushing, shredding, separation or disassembly
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Processing Of Solid Wastes (AREA)
Description
-1- DELAMINATION PROCESS The present invention relates to a process for recycling electronic scrap material such as optical recording media, for instance CDs and DVDs. In part the process involves delamination of electronic scrap material in order to recover the constituent components of it.
oIn the specification the term "comprising" shall be understood to have a broad meaning N similar to the term "including" and will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step 0 o or group of integers or steps. This definition also applies to variations on the term "comprising" such as "comprise" and "comprises".
The use of optical recording media such as CDs and DVDs has increased enormously in recent years with applications in the computer and audio/visual entertainment industries.
These media typically include a metal, such as aluminium and/or precious metals (typically gold or a mixture containing gold) provided on a polymeric substrate such as a polycarbonate. Typically the metal is provided on the polymeric substrate as a thin metallic film. A protective layer is usually formed on the outer surfaces, and acrylates such as polymethyl (meth) acrylates are commonly used in this respect. These optical recording media have a relatively short life of only a few years as they may become superseded or outdated. This leads to a considerable waste stream. Furthermore, there is a waste stream generated at the time of manufacture due to strict quality control standards: typically up to of manufactured product is rejected. Disposal of such waste is an increasing concern and recycling techniques are being investigated. Similarly other electronic scrap materials including precious metals and plastics are becoming increasingly available, and disposal of them is an important consideration also. In this specification the term "electronic scrap material" is used to embrace all such materials, including optical recording media such as CDs and DVDs.
Known processes for recycling electronic scrap material include smelting and chemical dissolution treatments that are primarily directed at recovering precious metals. Such methods tend to be damaging to any associated plastic material and, furthermore, the disposal of the plastic material can lead to environmental problems. Accordingly, chemical recycling methods tend not to be sympathetic to the environment.
O -2-
O
O
'I US Patent No. 5,306,349 assigned to Sony Music Entertainment Inc discloses a method for removing lacquer and aluminium coatings from the polycarbonate substrate of compact discs. This method uses an alkaline solution and the application of ultrasonic energy to compact discs immersed in this solution. Such treatments are not satisfactory when gold is present. Furthermore, the treatment could degrade the polycarbonate plastic.
O O O Recycling methods which rely on physical rather than chemical mechanisms have also been applied. For example, attempts have been made to remove a metallic layer from a 0 o polymeric substrate by slicing or shaving techniques. However, with such techniques the throughput can be relatively low and thus uneconomic where a large number of articles are to be recycled. Additionally, for security reasons, manufacturers sometimes choose to cut articles to be recycled g. CDs and DVDs) into pieces prior to transportation to a recycling facility. Techniques such as slicing and shaving cannot be applied practically to the articles in cut form.
Clearly therefore, it would be advantageous if a process could be devised for recycling an electronic scrap material which does not involve hazardous or potentially harmful chemicals and which is thus environmentally friendly, has high throughput and does not rely on the material to be recycled being in unitary form. Accordingly, the present invention provides a process for recycling an electronic scrap material comprising a metal provided on a polymeric substrate, which method comprises: milling flaked electronic scrap material with a bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; adding water to the milled material and separating the flakes of cleaned polymeric substrate from metal-containing material; dewatering and drying the flakes of cleaned polymeric substrate; and treating the metal-containing material to recover the metal.
The method is easy to perform and economic in practice. Moreover, it has been found that the polymer component it is desired to recover does not significantly degrade during the recycling process so that production of a high grade recycled product may be achieved.
WO 01/85414 PCT/AU01/00538 -3- In the present specification the term milling is used to denote any process by which attrition of the surface of the flakes of scrap material by contact with the bead impact material may be achieved. Such attrition removes of surface layer(s) of the scrap material and is a fundamental aspect of the present invention. In the context of the present invention the terms milling and attrition may be used interchangeably in addition to their usual meanings in the particle science industry.
The scrap material to be milled is in flake form. This means that the scrap material, for example a CD or DVD, is cut into individual flakes. This may be achieved using a conventional shredding machine or granulator. Ideally shredding/granulation cuts the material cleanly without any bending or distortion so that the resultant flakes are planar (assuming the original unitary material is planar). Bending or distortion of the scrap material during shredding/granulation can lead to metal smearing of the polymeric substrate material and/or may reduce the efficiency of the subsequent milling operation due to shielding effects.
The scrap material may be cut into flakes at the intended site of recycling or it may be supplied to the site in flake form. Thus, the process of the invention may include as preliminary steps the transportation of electronic scrap material to a flaking station followed by cutting the material into flakes. The flakes may then be transported to a recycling station where subsequent processing is carried out in accordance with the steps of the invention already described. If the scrap material is provided as is to the site where recycling is to take place, flake preparation will obviously be required prior to the subsequent processing. It is envisaged that in practice the scrap material would be supplied to a recycling facility in flake form. Depending on the flake size, further cutting of the flakes may be required prior to processing.
In an embodiment of the invention the flake size prior to milling is usually in the range 1 to for example 1 to 15mm, preferably 4 to 8mmn and more preferably 4 to 6mm. The optimum flake size will depend upon such factors as the size of the bead impact material used in the milling step. If the flake size is too small, valuable polymeric material may be lost as fines in downstream process steps.
WO 01/85414 PCT/AU01/00538 -4- The flake size has implications with respect to the size of bead impact material used in the milling step. Thus, for relatively large flakes, milling may be optimised using a different size bead impact material when compared with the size of bead impact material most suitable for attrition of smaller flakes.
In a preferred embodiment, the flake size falls within a narrow distribution so that a correspondingly narrow distribution of size of bead impact material may be used in the milling step. For example, it is preferred that at least 50 wt%, for instance at least 75 wt% of flakes have a size of 4-8mm, and preferably 4-6mm. It will be appreciated however that a given batch of flakes to be treated may well have a broad distribution of flake size, and to optimise the milling step, bead impact material having a range of particle sizes may be used.
In an embodiment of the invention the flakes to be processed may include a distribution of flake size such that it will be most efficient to mill flakes above a predetermined size with a first size of diameter bead impact material and to mill flakes at or below the predetermined size with a second size diameter of bead impact material. This embodiment of the present invention would thus comprise the following steps: milling flaked electronic scrap material that is above a predetermined flake size with a first size diameter of bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; milling flaked electronic scrap material that is at or below the predetermined size with a second size diameter of bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; adding water to the milled material and separating the flakes of cleaned polymeric substrate from metal-containing material; dewatering and drying the flakes of cleaned polymeric substrate; and treating the metal-containing material to recover the metal.
WO 01/85414 PCT/AU01/00538 In this embodiment, the predetermined size is typically about 3mm. The first size of bead impact material is usually greater than 1 000um and the second size of bead impact material is usually less than 1000 m. The first attrition or intensive shear stage generally leads to 80-90% removal of metal from the polymeric substrate.
As a further feature of this embodiment, prior to the first milling step, the process may comprise: transporting a waste stream of electronic scrap material to a flaking station; dividing the material into flakes at the flaking station; and transporting the flakes to a milling station.
For the typical flake size contemplated (1 to 20mm) the milling step may be performed using a bead impact material having a particle size as low as 50 um. If the flake, or a significant proportion of the flake (for instance in excess of 50 has a particle size of the particle size of the bead impact material may be as high as 3mm. The function of the bead material is to remove by attrition the metal, and any additional layer(s) overlying the metal, and one skilled in the art would be able to select a suitable bead impact material size, or distribution thereof, based on this intended function and the following description of other relevant operational parameters.
As bead impact material any material serving the intended function of removing the metal, and any additional layer(s) overlying the metal, may be used. Thus, the bead impact material should have a suitable surface hardness. Interactions between individual flakes may also contribute to the attrition process. For optimum effect it is preferred that the bead impact material is in the form of particles having irregular surfaces. It is also preferred that the bead impact material has a roughened rather than smooth surface. As the milling step takes place in water, the material should also be suitably stable in water. The process of the invention will also typically be carried out at elevated temperature and it follows from this that the bead impact material should also have the necessary integrity at the maximum temperature at which the process is performed.
Examples of bead impact material which may be used include plastics, silicon-containing WO 01/85414 PCT/AU01/00538 -6materials, ceramics and metal powders. Examples include pumice, sand, powdered glass, diatomaceous earth and silicon carbide. Such materials are commercially available. It is also possible to make use of commercially available scouring agents, such as Ajax and Jif, which include abrasive particles in a carrier fluid/paste. It is preferred to use pumice having a particle size of about 300gun or less or silica having a particle size of about 150gm or less. The use of metals as bead impact material can sometimes lead to discolouration of the polymeric substrate due to smearing. Ceramic materials exhibit excellent abrasive properties although this should be counterbalanced with their tendency to be brittle. In an embodiment of the invention it is possible to use the polymeric material itself, possibly recycled from the process described herein, as the bead impact material.
Thus, in CDs and DVDs where the polymeric substrate is s polycarbonate, the bead impact material may be recycled polycarbonate.
In an embodiment of the invention it is preferred that the density of the bead impact material is not too dissimilar from that of the polymeric substrate it is desired to recover. The effect of this is that there is enhanced mixing and dispersion of the bead impact material and the flake. If the density of the bead impact material and polymeric substrate is substantially different, partitioning the two may occur resulting in less effective attrition. The size of the bead impact material and the flake may also be matched to enhance mixing and dispersion of the two.
The quantity of bead impact material may vary based on the amount of flake material present, and this will affect the rate of attrition. Thus, where the proportion of bead impact material is high relative to the amount of flake present, the rate of removal of metal, and any overlying layer(s), is correspondingly high. However, the rate of attrition should also be balanced with the rate of wear of the material and/or apparatus that will likely ensue.
Typically, the weight ratio of bead impact material to flake is 1:30, for example 1:20. In practice the weight ratio chosen will be influenced by the desired process time which in turn may be influenced by things such as electricity costs.
WO 01/85414 PCT/AU01/00538 -7- An important aspect of the invention is that the milling step takes place in the presence of water. The water functions as a lubricant and heat transfer medium as well as aiding transport of the milled products. Without wishing to be limited by the following hypothesis, it is believed that the high intensity attrition due to the bead impact material leads to rapid distortion and heating of the flake at the interface between the various layers present, for example at the metal/polymeric substrate interface, leading to loss of adhesion and delamination. It can also be likened to the cutting of oxidised paint for surfaces with a car polish. Typically, the weight ratio of water to flake is from 1:3 to 3:1 and, preferably, 1:1. If the proportion of water is much in excess of this, the process of the invention works less efficiently.
The process of the invention may be carried out under ambient conditions of temperature and pressure, although it will be appreciated that the milling step will itself cause a temperature increase due to frictional interactions. Typically, for a given process time where lower temperatures are used more bead impact material is required. It is possible to carry out the process at elevated temperature and, in part, this may be achieved by using heated water in the milling step. Indeed, it has been found that elevated temperature either imposed externally, for instance by use of hot water and/or thermal jacketing, or generated in-situ is associated with acceleration of the attrition process. In the case of CDs which have an acrylate outer layer overlying the metal layer, the use of elevated temperature also advantageously lowers the integrity of the acrylate layer thereby facilitating its removal.
At elevated temperature it is believed that the acrylate becomes tacky/sticky and this property may lead to enhanced removal of the underlying metal layer when the acrylate layer is itself removed. The process of the invention may therefore be carried out at elevated temperature provided that the polymeric substrate it is desired to recover is not adversely affected. Thus, where the polymeric substrate is a polycarbonate the process may be carried out at a temperature of, for example, up to 120 0 C (in which case the process must be carried out under pressure). Where the process is carried out at atmospheric pressure the maximum temperature will be 100 0 C. In determining the temperature at which the process is carried out the temperature increase due to the milling operation itself must be accounted for.
WO 01/85414 PCT/AU01/00538 -8- Milling takes place in any suitable apparatus which is capable of causing high shear between the flakes and bead impact material. Thus, a high shear mixer, a stirred attrition mill, a peg mill mixer or a bead mill may be used. The duration of milling will vary depending upon such factors as the shear imparted by the mixer, the type and proportion of bead impact material, the flake size and the temperature, and may be determined on a caseby-case basis for optimum results.
Prior to milling, it is preferred that the flakes are washed in an aqueous medium containing a detergent or surfactant suitable to remove any particulate and absorbed contaminants from the flake surface.
Subsequent to milling water is added to the flakes of polymeric substrate material. This effectively washes the flakes to remove any products of attrition and the bead impact material. Preferably, the flake is subjected to shear washing with water. Water used in this step may be recycled to the milling step in order to minimise loss of potentially valuable components.
The flakes of washed polymeric substrate are then separated from metal-containing material, and other materials such as derived from any overlying layer(s), using conventional techniques. The separated flakes of polymeric substrate may then be dewatered and dried by conventional techniques. The polymeric substrate is now in a form which may be useful for further applications. Depending upon the grade of the resulting polymer, this may include re-use in an electronic material such as a CD or DVD.
Alternatively, the polymeric substrate material may be used in applications where the grade of the material is not as critical.
The metal-containing material is treated to recover the metal. This may be achieved using a thickener, such as a Lamella thickener, which allows the metal solids to settle and flowover water to be removed. A conventional flocculating agent may be used in this step.
The metal may then be recovered by filtration techniques such as by use of a pressure filter, drum filter or belt filter. A cake of metal is obtained.
WO 01/85414 PCT/AU01/00538 -9- In the case of CDs and DVDs the scrap electronic material includes primarily polycarbonate polymers, aluminium and gold. However, a number of other materials may also be present. These include various adhesives, polymeric materials, lacquers and printing inks. To maximise the value of the polycarbonate polymer it is important and preferred that in its recovered state it is free from contaminants and also that its molecular weight has not been adversely reduced by the recovery process. Any undesirable reduction in molecular weight may be remedial increasing the molecular weight in accordance with conventional techniques. It is less important to have the gold free from other materials as the weight concentration of the gold is relatively low, typically only 1 00ppm.
In an embodiment of the invention the process may be used to recover polycarbonate and metal from a CD or DVD. CDs typically have a substrate layer of polycarbonate which is coated on one side with a metal backing layer (usually aluminium). The CD also includes as an outer layer over the metal backing layer an acrylate layer. The present invention may be applied to strip off the layer of acrylate and the layer of metal in order to isolate the polycarbonate. The metal may also be recovered. DVDs may be single-or double-sided.
In the double-sided version a layer of metal, typically gold or a gold alloy, is sandwiched between two substrate layers of polycarbonate and acrylate layers may be provided as outer layers on the respective polycarbonate substrate layers. The metal is usually bonded to the polycarbonate layers with an adhesive. In order to access the metal layer it is necessary to delaminate the DVD structure. Cutting the DVD into flakes usually initiates this and subsequent milling will further it. The polycarbonate may be isolated as described using milling/attrition.
As a practical example when recycling a CD or DVD of the type described it is preferred that the CD or DVD is cut into flakes having an even distribution of particle size of about 6mm. The weight ratio of water:flake used is typically 1:1 and the process temperature about 80"C. As bead impact material silica powder with a maximum particle size of 150pm or polycarbonate pellets with a particle size of 1 to 2mm may be used. In either case the weight ratio of the bead impact material to flake is approximately 1:20.
WO 01/85414 PCT/AU01/00538 Although readily applicable to what may be regarded as conventional electronic materials, the invention may be applied to any scrap material in which a metal is provided on a polymeric substrate. For example, the invention may be used to recycle aircraft windows and vehicle headlight reflective backings.
The invention will now be illustrated by the following non-limiting examples. In the examples estimates of sample cleanliness were assessed visually with the aid of an optical magnifier.
Example 1 100 of DVD discs were reduced to chipped flakes with maximum dimension of 10mm in a mechanical flaker. The chips were then chemically cleaned in a washing station to remove surface contaminants. The material was then separated by size to above and below 3mm using a sieve. The portion less than 3mm was milled using Ballotini media (glass beads less than Imm in diameter) for one hour. The portion greater than 3mm was milled separately using Ballotini media. The cleaned flakes were then fed into a stirred bead mill, where they were milled for 15 minutes with Ballotini media. Surprisingly, it was estimated that at least 80% of the adhering surface layer had been removed by the action of the beads and the now heated water.
The material from each of these millings was separated on the basis of size into gold rich and polymer rich fractions. The polymer fraction was dewatered and dried to give a high purity compounding grade of polycarbonate.
Example 2 0.2kg of 6mm flakes of a CD and 0.24kg of water (heated to 80 0 C) were milled using a peg impeller in a 90mm diameter container surrounded by a 110mm diameter container as a water jacket. The bead impact medium was O1g pumice having a maximum particle size of approximately 300[jm. The impeller was operated at approximately 1500 rpm. Over the course of an hour a temperature rise of 8°C was observed (the water temperature initially fell to 72 0 After as little as a quarter of an hour the. flakes were estimated to be WO 01/85414 PCT/AU01/00538 -11- 99% clean.
Example 3 Example 2 was repeated except that the container was 88mm diameter, the impeller operated at 2095rpm and the test run for 60 minutes. The temperature of the water after addition to the container was recorded at 35 0 C rising to 65 0 C after a total of 60 minutes. A sample taken at 30 minutes was estimated to be 97% clean. A sample taken after minutes was estimated to be 99% clean.
Example 4 Example 3 was repeated except that the pumice was replaced with 10g silica having a maximum particle size of 150pmn. After 15 minutes the water temperature was 75 0 C rising to 87 0 C after a further 15 minutes. Samples were taken at 5 and 30 minutes and were estimated to be between 95 and 97% clean.
Example Example 3 was repeated with the water temperature being 72 0 C after 5 minutes rising to 95 0 C after 15 minutes. A sample taken after 5 minutes was estimated to be 99% clean.
Example 6 0.lkg of 6mm flakes of a DVD and 0.28kg of water were milled using a peg impeller in an 83mm PVC container using 5g of pumice having a maximum particle size of 300Am.
After 5 minutes the temperature was 35 0 C rising to 65 0 C after a total of 30 minutes.
Samples taken at 15 and 30 minutes were estimated to be at least 96% and at least 98% clean respectively.
As an independent aspect of the present invention it is possible for the flakes of scrap material to function as the bead impact material, i.e. it is not essential to include any extraneous abrasive in order to achieve the desired attrition. The present specification may be understood with this in mind. This is particularly useful when recycling CDs.
WO 01/85414 PCT/AU01/00538 -12- Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.
Claims (15)
1. A process for recycling an electronic scrap material comprising a metal provided on a polymeric substrate, which method comprises: milling flaked electronic scrap material with a bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; adding water to the milled material and separating the flakes of cleaned polymeric substrate from metal-containing material; dewatering and drying the flakes of cleaned polymeric substrate; and treating the metal-containing material to recover the metal.
2. A process according to claim 1 wherein the electronic scrap material is a CD or DVD.
3. A process according to claim 1 or claim 2 which is carried out at a temperature from ambient up to
4. A process according to claim 1 or claim 2 which is carried out at a temperature from ambient up to 120 0 C. A process according to any one of the preceding claims wherein the weight ratio of water to flake is from 1:3 to 3:1.
6. A process according to claim 5 wherein the weight ratio of water to flake is 1:1.
7. A process according to any one of the preceding claims wherein the flake size is 1 to
8. A process according to claim 7 wherein the flake size is 4 to 8mm.
9. A process according to any one of the preceding claims wherein the bead impact material is selected from plastics, silicon-containing materials, ceramics and metal powders.
10. A process according to any one of the preceding claims wherein the bead impact WO 01/85414 PCT/AU01/00538 -14- material is pumice or silica.
11. A process according to claim 10 wherein the pumice has a particle size of 300g-pm or less.
12. A process according to claim 10 wherein the silica has a particle size of 1504m or less.
13. A process according to any one of the preceding claims wherein the bead impact material is recycled polymeric substrate.
14. A process according to any one of the preceding claims comprising the steps: milling flaked electronic scrap material that is above a predetermined flake size with a first size diameter of bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; milling flaked electronic scrap material that is at or below the predetermined size with a second size diameter of bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; adding water to the milled material and separating the flakes of cleaned polymeric substrate from metal-containing material; dewatering and drying the flakes of cleaned polymeric substrate; and treating the metal-containing material to recover the metal. A process according to claim 14, which comprises, prior to the first milling step: transporting a waste stream of electronic scrap material to a flaking station; dividing the material into flakes at the flaking station; and transporting the flakes to a milling station.
16. A process for recycling an electronic scrap material comprising a metal provided on a polymeric substrate, which method comprises: milling flaked electronic scrap material with a bead impact material in the presence of water to produce flakes of cleaned polymeric substrate; adding water to the milled material and separating the flakes of cleaned polymeric substrate from metal-containing material; IO 0 Cl dewatering and drying the flakes of cleaned polymeric substrate; and Streating the metal-containing material to recover the metal, wherein the bead impact material comprises flakes of scrap electronic material.
17. A process for recycling an electronic scrap material comprising a metal provided on a polymeric substrate substantially as herein described in the specification 0 0 with particular reference to the examples. O DATED THIS THIRTEENTH DAY OF JANUARY 2006 C METSS.org LLC BY PIZZEYS PATENT AND TRADE MARK ATTORNEYS
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPQ7471 | 2000-05-11 | ||
| AUPQ7471A AUPQ747100A0 (en) | 2000-05-11 | 2000-05-11 | Delamination process |
| PCT/AU2001/000538 WO2001085414A1 (en) | 2000-05-11 | 2001-05-11 | Delamination process |
| AU5600001A AU5600001A (en) | 2000-05-11 | 2001-05-11 | Delamination process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2001256000A1 AU2001256000A1 (en) | 2002-02-07 |
| AU2001256000B2 true AU2001256000B2 (en) | 2006-03-02 |
Family
ID=25631080
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2001256000A Ceased AU2001256000B2 (en) | 2000-05-11 | 2001-05-11 | Delamination process |
| AU5600001A Pending AU5600001A (en) | 2000-05-11 | 2001-05-11 | Delamination process |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU5600001A Pending AU5600001A (en) | 2000-05-11 | 2001-05-11 | Delamination process |
Country Status (1)
| Country | Link |
|---|---|
| AU (2) | AU2001256000B2 (en) |
-
2001
- 2001-05-11 AU AU2001256000A patent/AU2001256000B2/en not_active Ceased
- 2001-05-11 AU AU5600001A patent/AU5600001A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU5600001A (en) | 2001-11-20 |
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| FGA | Letters patent sealed or granted (standard patent) | ||
| PC | Assignment registered |
Owner name: GEO-TECH HOLDING COMPANY, LLC Free format text: FORMER OWNER WAS: METSS.ORG LLC |
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| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |